Ebola viruses are important emerging and biodefense pathogens for which there are no approved efficacious therapeutics. The overarching goal of the center will be to study Ebola viral RNA-dependent RNA polymerase complex and its interaction with proteins and RNA using structural and functional studies and to identify novel host factors that are critical for viral replication. The characterization of the viral RNA synthesis machinery by this interdisciplinary project will provide insight in to Ebola virus biology and identify new therapeutic targets. This is a multi-investigator collaborative research center with research conducted at several sites. The Administrative Core will coordinate advances in the research among the scientific components (Projects 1, 2, and 3; Core B and C). To ensure that the progress of this integrated research program will be maximized, the Administrative Core will be responsible for the following roles: Coordinate: weekly (at a minimum) teleconferences between the PIs of the research projects and cores; monthly (at a minimum) scheduled web- based interlab meetings to exchange and critique data; and annual Meeting among members of all participating groups, to be held at one of the participating sites. These meetings will facilitate reagent and scientific exchanges between the different laboratories. The Administrative Core will also coordinate annual meetings between the investigators and the External Advisors to assess scientific progress and to receive critical evaluations on the performance and future directions of the P01 project. In addition, the Administration will coordinate budget usage and establish a ?Core Usage Committee? to ensure that the research projects are well supported by the scientific cores. It will assist the investigators with preparation and submission of annual progress reports to the NIH; maintain a web site for data dissemination in connection with this project. The Administrative Core will provide support for efforts to recruit and educate research fellows, graduate and medical students in the field of virus-host interactions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
1P01AI120943-01A1
Application #
9149556
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2016-07-07
Budget End
2017-06-30
Support Year
1
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Dashti, Hesam; Wedell, Jonathan R; Westler, William M et al. (2018) Applications of Parametrized NMR Spin Systems of Small Molecules. Anal Chem 90:10646-10649
Johnson, Britney; McConnell, Patrick; Kozlov, Alex G et al. (2018) Allosteric Coupling of CARMIL and V-1 Binding to Capping Protein Revealed by Hydrogen-Deuterium Exchange. Cell Rep 23:2795-2804
Holze, Cathleen; Michaudel, ChloƩ; Mackowiak, Claire et al. (2018) Oxeiptosis, a ROS-induced caspase-independent apoptosis-like cell-death pathway. Nat Immunol 19:130-140
Warfield, Kelly L; Howell, Katie A; Vu, Hong et al. (2018) Role of Antibodies in Protection Against Ebola Virus in Nonhuman Primates Immunized With Three Vaccine Platforms. J Infect Dis 218:S553-S564
Su, Zhaoming; Wu, Chao; Shi, Liuqing et al. (2018) Electron Cryo-microscopy Structure of Ebola Virus Nucleoprotein Reveals a Mechanism for Nucleocapsid-like Assembly. Cell 172:966-978.e12
Knoverek, Catherine R; Amarasinghe, Gaya K; Bowman, Gregory R (2018) Advanced Methods for Accessing Protein Shape-Shifting Present New Therapeutic Opportunities. Trends Biochem Sci :
Johnson, Britney; VanBlargan, Laura A; Xu, Wei et al. (2018) Human IFIT3 Modulates IFIT1 RNA Binding Specificity and Protein Stability. Immunity 48:487-499.e5
Klein, Roger D; Shu, Qin; Cusumano, Zachary T et al. (2018) Structure-Function Analysis of the Curli Accessory Protein CsgE Defines Surfaces Essential for Coordinating Amyloid Fiber Formation. MBio 9:
Hung, Putzer J; Johnson, Britney; Chen, Bo-Ruei et al. (2018) MRI Is a DNA Damage Response Adaptor during Classical Non-homologous End Joining. Mol Cell 71:332-342.e8
Johnston, Adam B; Hilton, Denise M; McConnell, Patrick et al. (2018) A novel mode of capping protein-regulation by twinfilin. Elife 7:

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